Hydrogen thyratron



Nov. 7, 1950 G. J. REILLY ET AL HYDROGEN THYRATRON 5 Sheegts-Sheec 1 Original Filed Aug. 3, 1945 FIG.|

INVENTOR. WILLIS E. HARBAUGH GERARD J- REILLY BY QX fl m fl FIG.4

Nov. 7, 1950 G. J. REILLY ETAL 2,528,547

HYDROGEN THYRATRON' Y Original Filed Aug. 5, 1945 5 Sheets-Sheet? FIG.9

-FIG.6

IN VEN TOR.

WILLIS E. HARBAUGH GERARD J. REILLY.

A/fornqy Nov. 7, 1950 ca. J. REILLY ET AL 5 54 HYDROGEN THYRATRON Origipal Filed Aug. 3, 1945 5 Sheets-Sheet 3 INVENTOR. WILLIS E. HARBAUGH GERARD J. REILLY fl for/lg Nov. 7, 1950 G. J. REILLY HAL 5 5 HYDROGEN THYRATRON Original Filed Aug. 5 19 45 5 Sheets-Sheet 5 FIG. l4

FIG. I5

CURVE FOR ZIRCONIUM HYDRIDE TEMPERATURE IN DEGREES CENTIGRADE IOO CURVE FOR TITANIUM HYDRIDE wmwmwmm 7 5 3 2 mZOmQE Z- mmDwwmma TEMPERATURE IN DEGREES CENTIGRADE INVENTOR.

wu.us E. HARBAUGH GERARD J. REILLY BY fl/wmf $12M flff'orflf] in the tube.

Patented 7,' 1950 UNITED- STATE 5 PATENT OFFICE 71 HYDROGEN THYRATBON Gerard J. Reilly, Rumson, and Willis E. Harbaugh, Fair Haven, N. J.

Original application August 3, 1945, Serial No.

Divided and this application September 8, 1949, Serial No. 117,484

1 Claim.

(Granted under the act of March 3, 1883, as amended April 30, 1928; 370 O. G. 757) The invention described herein may be manufactured and usedby or forthe'Government for governmental purposes; without the me of any royalty thereon.

This application is a division of application Serial No.'608,827, filed August 3, 1-945, under the same name and title.

payment to This invention relates to gas-filled thermionic tubes andv more particularly to their methods of manufacture and to 'certain structural improvements which embrace the characteristics and life of these gas-filled tubes o'fthe type which use hydrogenas the ionizable conducting medium.

a This application has matured on February 21,1950, into Patent No.-

Inthe prior-art it has been a well established r practice ,to use mercury vapor. asap ionizable mediumwithin the gas-filled tubes because of the low voltage drop obtainable with the mercury arc,

this low voltage drop contributing to high efifi- .ciency of the tubes, and because of the ease. of maintaining constant the required pressure with;-

The latter requirement is usually 1 satisfied byjintroducing some excess" mercury metal into the evacuated vessel of the tubefthis excess maintaining the pressure constant at any given operating temperature of the tube. Thus the mercury-filled tubes are devoid of gas "cleanup difliculties So longIas'j-ambient temperature changes donot exceed approximately ,120 C. change from room temperature, Since mercury cury vapor being so high that the'greater degree 7 of ionization of the mercury vapor, produces the expense of this slightly higher voltage drop -0I1e can obtain stable operation of the tube over a much wider ambient temperature range. This is indeed the case when hydrogen is used as the conducting medium. Moreover, hydrogen has an added advantage of having a shorter time of deionization, which is a very desirable feature in many applications of the gas-filled tubes. It has been discovered'however, that substitution of hydrogen for mercury may result in the socalled gas clean-up phenomenon, the hydrogen in the tube vessel being gradually absorbed by the elements of the tube thereby shortening the v useful life; of the tube.

This invention discloses the methods of pro- {viding hydrogen-reservoirswithin the structure ofthe tube so that the hydrogen clean-upphenomenon iseliminatedaltogether and the-useful life of the tube does notdepend any longer on the supply of hydrogen According to the invention various hydrogen-absorbing elements or materials, are used in constructing the tube, and

these'elements ormaterials are saturated with hydrogen-prior to sealing of the glass vessel. 7

7 According to another embodimentof the. in-

"vention the hydrogen reservoir is provided in a .formof a capsule containing a hydridefiof the above elements or materials which can be heated bymeans of an electric heating .coil to that temperature which maintains the desired hydrogen pressure constant.

- ,t'fIt is: therefore an object of this invention to flash-overs and sustained arcs. Thus when large ambient temperature, variations, such "as :those encountered in connection with aircraft or military use, are-anticipated, it becomes necessary ,to substitute some medium formercury which provide a hydrogen-filled thermionic tube with afireservoir of hydrogen which is capableof replenishing free hydrogen in the tube.

,An additionalobject of this invention 15 to prov videareservoir of hydrogen for a hydrogen filled thermionic tube, thisreservoir being in a form of a. hydride deposited on som'e of the metallic elements of the tube. f

' Still another object of this invention is to provide areservoir of hydrogen for a hydrogen-filled thermionic tube, the reservoir being in-a term of a heated'c'apsule.

These andother objects of the inventionwill :be more clearly understood from the following detailed description and the accompanying draw-- will be less sensitive to large fluctuations in the ambient temperature. One of the more suitable substances is hydrogen. Hydrogen has a somewhat higher are voltage drop, but this higher ,voltage drop: becomes avery minor factor if at ings in which;

Figure 1 isan elevational View of a hydrogen filled thermionic tube, or thyratron,

Figure 2 is the enlarged cross-sectional view of the cathode of the thyratron illustrated in Fig. 1, 1

Figure'3 is an explanatory figure, Figures 4 and 5 are the enlarged cross-sectional metals.

Figure 13 illustrates time vs. pressure curves of a mega-watt thyratron when it is turned on.

In the introductory part of the specification it has been stated that since mercury vapor is readily condensible at the low pressures and temperatures, the mercury tubes are sensitive to ambient temperatures. The same difiiculty may 7 known as occlusion.

4 2. Indefinite metallic hydrides. These form solid phases Whose composition varies with external conditions of temperature and hydrogen pressure, somewhat similar to absorbants of colloids. An example is the zirconium-hydrogen alloy. They will be called physical hydrides, although some have a definite formula when the maximum hydrogen is combined, and others have an undetermined formula resembling a solid solution of the hydrogen in the metal and sometimes Since actual formulas of such previously undetermined compoundsare established from time to time, it may be reasonable to assume that the now undetermined formulae will also be established; in any case the compositions are commonly known as hydrides.

T|able.A. Werners periodic table modified to show the relation of the elements to hydrogen not have any appreciable effect. onthe hydrogen pressure maintained by the selected hydride. The

controlling factors in selecting the hydrides will become more apparent from the discussion that isto follow.

It is known that hydrogen unites, physically and chemically with most elements forming hyd'rides. The term hydrides, in the "broadest sense, includes the chemically combined elements such as BaI-Iz and indefinite, physical, metallic hydrides such as TaI-Is.

Compounds of the non-metals and m etalloids,

in which hydrogen seems to'play the role'of a positive univalent element, while the other element behaves, as a negative or a non-metallic element, are usually, although not always, more stable than the hydrides of the metals, and'there- H He Li Be B o YN o F Na Na Mg Al Si P s 01 A K Ca s 'li v Cr Mn Fe 00 Ni Cu Zn Ga Ge As Se Br Kr Rb Sr Y Zr Nb Mo Ru Rh Pd Ag Cd In Sn Sb Tc I x f cs Ba n iit gfi s Ta W 0s n" Pt 'Au Hg Tl T Pb i Ra ThU h side of the table. The compounds with'the nonmetals andjmetalloids are confined to a groupbn theextrerne'right, also marked oil witha heavy line on the right side of the table'an'dare not considered here as explained above; The center part of the table between the heavy lines, is occu-' pied by the metals, which form the indefinite metallic hydrides which ar class 2 The elements which combine as physical yfgrouped above 'in drides thus-form a center group with sub-groups on the left and right. The sub-group on the right represents the previously mentioned on-rhetals and 'metali'oids which form more stable-hydrides fore represent poor sources of hydrogen for the I intended purpose. Sincethere are available more su table sources of hydrogen among metallic hydrides, the discussion of the compounds of the non-metals and metalloids will be omitted altogether.

Difierent products of the action of hydrogen on metals maybe arranged in two classes:

1. Compounds of the alkali and alkaline-earth These compounds are crystalline and are stable enough to be volatile without much decomposition in an atmosphere of hydrogen at comparatively low temperatures. They are hysent definite chemical compounds.

.drides proper, being related to the chlorides and I are less suitable for theintended'purpose.

. 'Among the elements combining as physical hydrides, which form the center group in'the Werners table, the following elements forni'the most suitable 'hydrides: zirconium; titanium; tantalum; thorium, anol urani'um'. Although numerous other elements from the center group are capable of occluding'large amounts ofhydro'gen, Which'in some instancesexceeds the amount absorbed by. the above mentioned elements (a'leading example is palladium),-the dissociation temperature'of some of these hydrides, at the desired pressure,- is so low thatthey-do not represent most suitable sources of hydrogen and for this reason will not be discussed in. this specification. l The rare earth metals, although they also form hydrides, are, with the exception of cesium,-not readily available elements, and for this reason do not represent practical sources of hydrogen'for the intended use.

' In the sub-group on the left side, which includes the previously mentioned compounds of the alkali and alkali-earth metals of the first cla barium, strontium and calcium are the 5.. 'most suitable elements forming that type of hydrides which have the dissociation temperature and pressure equilibriums which are the most suitable to act as the sources of hydrogen, with barium forming one of the more efiective hydrides for the intended use among the selected group.

In the table, among the physical hydrides, 'zirconium is one of the more efiective absorbers whose dissociation temperature, creating the desired pressure, isisufficiently high to make it, for practical purposes, insensitive to the relatively large fluctuations of the ambient temperature. Because of these physical characteristics of the zirconium hydride, it represents an especially effective reservoir'of hydrogen, this reservoir taking the form of a physical hydride in this instance. However, zirconium hydride, as well as numerous other physical hydrides, is brittle, and therefore can not be used independently for constructing the structural elements of the tube. It may be used nevertheless as a source of hydrogen if it is deposited in the known manner in the form of a very fine metallic powder, metallic layer, or spongy metallic layer, on the surfaces of the structural elements of the tube, and especiallyon those elements which attain sufiiciently high temperature to produce the necessary hydrogen pressure in the vessel of the tube, the temperature of these elements thus being the sole factor controlling the hydrogen pressure in the tube, as long as there is sluifi'cient of amount of hydride material for the volumetric displacement of the vessel of the tube. This is also thecase even if there is a gradual absorption and adsorption of a hydrogen taking place by any other elements of.

the tube since any lowering of the pressure is simultaneously compensated by the liberation of additional hydrogen by the metallic hydride according to the well known phase rule.

The same procedure of coating metallic structural elements is also applicable to the hydrides of the first class. I Y

1 the cathode.

Thus, in this form of the invention, the struc-" turalelements of the tube, when heated to their operating temperatures, furnish the necessary source of heat for heating the selected hydride to that dissociation; temperature which creates the desired hydrogen pressure within thevessel of the tube according to the phase rule, and this pressure remains constant as long as the temperature of the hydride remains constant.

According to another embodiment'ofthe ini vention, the hydrides, either of the first or second way of an example in connection with a one megawatt thyratron and the selected hydride will be zirconium hydride of the second class.

Referring to .Fig. 1, a glass vessel Ill is constructed in well-known manner with an anode lead 12 emerging from the vessel through an j upper glass seal I4, this seal holding an anode 15 in spaced relationship with'respect to grid elements l6 and; 11., Thegrid element including mesh sleeve 25 is fastened with its upper portion to the upper glass seal by means of a collar l8, the lower portion of the grid being connected to a cylinder H! which acts as a support for the grid as well as a conducting element for' connecting the grid to a lead-in wire 20 connected to prong 48. Cylinder I9 is supported by wires 2| and 22 embedded in a glass press 23. Cylinder l9 also acts as a heat shielding element for the cathode of the thyratron. Only an external heat shield 24 and a bafile 45 of the'cathode are visible in Fig. 1, the enlarged cross-sectional view of the cathode being illustrated more fully in Fig. 2. It consists of a cathode cylinder 26 provided with a plurality of vanes 21 which increase the emissive surface of the cathode. The inner surface of cylinder 26 and all surfaces of the vanes 2'! are coated with an electron emitting mixture of barium and strontium oxide. The cathode cylinder 26 is surrounded by a heater coil 28 which is coated with a refractory, insulating material such as aluminum oxide for insulating the coil from the cathode. The coil is connected by means of a conductor 29 and a lead-in wire 30 to 2. prong 3|, the opposite end of the coil being spot-welded to the upper rim of the cathode cylinder 2B.' The cathode cylinder rests on a hat 34 which in turn is supported by an intermediate bafiie 35 and the baffle itself is supported by a cathode base 36; the hat, the intermediate bafiie, and'the cathode base all have an opening for wire 29 as illustrated in the figure, these openings permitting the connection between the coil and the lead-in wire 30. Besides acting as a supporting means for the cathode, the hat, the intermediate battle, and the base, act as heat shields for theheater coil and In the vertical plane, the heater coil and the cathode are provided with an internal heat shield 31 and an external heat shield 24, these two shields representing two metallic cylinders. Base 36 is spot-welded to the external heat shield 24, the intermediate baflle is spotwelded to the cathode base 36, and hat 34 is spot-welded to the intermediate bafile 35. The upper portion of the cathode cylinder 36 is provided with straps 39 and 40 which are spotwelded tothe external heat shield 24. The upper structure of the cathode is provided with a heat shielding ring 4| and a battle ring 42, the

two being spot-welded together to each other and to the external heat shield 24. Rings 4! and 42 are provided with central openings 43 and 44 which allow the electrons to follow their path acts as a heat shield as wen as a baiilepreventingthe deposition of the electron emitting barium and strontiumoxides on the grid and'anode elements of the tube. The external heat shield 24 is supported by the wires 46 and 4! connected tov prong149of the thyratron; In addition to the nickel in which chemically pure nickel comprises approximately 99% and the remaining 1% should be relatively free of such impurities as copper, iron, manganese, magnesium and carbon which are to a considerable extent responsible for the'hydrogen clean-up phenomenon.

v Obtaining of nickel which is free of hydrogen absorption is oftendifficult and introducing of the hydrogen reservoir into the vessel simplifies 7 this problem to a very large extent since, as mentioned previously, even if there is any absorption of hydrogen it is compensated for by the hydride. Thus with the hydrogen reservoir available within the vessel it is also possible to use nickel which has a lower degree of purity.

The operating elements of the tube, such as cathode structure illustrated in Fig. 2, the grid elements iii-i8, shield l9, and anode I5, all have diiierent operating temperatures, and since it is the temperature that controls the amount of liberated hydrogen, and thus the pressure of the liberated hydrogen, the deposition of zirconium on any specific element or elements of the tube is controlled by the operating temperatures of that particular element or elements. Since the operating temperatures of the elements vary in different structures and types of tubes, no universal rule can be stated as to which particular element should be coated with zirconium. It is obvious that cathode cylinder 26 is always the hottest element in the tube, and when the highest degree of dissociation is desired for any particular tube, and the temperature of the cathode, such as cylinder 26, in Fig. 2, does not exceed the desired dissociation temperature, the cathode is the proper element to use for depositing zirconium. In Fig. 2, the deposition of zirconium wouldbe on the outer surface of cylinder 26 since its inner surface and vanes 21 are used for depositing barium and strontium oxides. ,Thus the electron-emitting oxides are deposited on the inner walls of the cylinder While zirconium is deposited on the outer wall, as illustrated in Fig. 5. Fig. 5 shows a portion of an enlarged cross-sectional view of the wall of cylinder 26 constructed according to this method. The center element 588, whichcorresponds to cylinder 28, is made of nickel, the inner layer 582 deposited on the nickel structure 550, represents an electron-emitting mixture of barium and strontium oxides, and layer 594, deposited on the outer surface of the nickel cylinder 503,,represents a layer of metallic zirconiumhydride which adheres-to nickel wall 569.. It is zirconium hydride 5% that acts as a reservoir of hydrogen in the illustrated structure.

1 In Imany instances the temperature of the cathode cylinder is too high for producingthe desired equilibrium pressure required for good tube performance and when this is the case it becomes necessary, to deposit zirconium prior to its hydro genation "on some other elements of the tube These eletioned elements.

Since dissociation of hydrogen follows the phase rule, the dissociation process in the majority of physical hydride is a reversible phenomenon with the result that when the operation of the tube is discontinued and the tube cools itself off to ambient temperature, the liberated hydrogen isabsorbed again by the metal. When the tube is operated at the. extremely low ambient temperatures, the initial hydrogen pressure, prior to turning on the tube, may be anywhere between zero and slightly above zero, but lower than the required hydrogen pressure for normal operation of the tube. Therefore, it becomes necessary to restore the hydrogen pressure before the tube may be operated as a gas-filled thermionic tube, and this restoration of the hydrogen pressure is accomplished simultaneously with the bringing up of the cathode temperature to the electron-emitting temperature, hydrogen gas being liberated by a hydride simultaneously with the heating cycle of the cathode cylinder 26.

It. is to be noted that the equilibrium pressure of hydrogen liberated by the hydrides is a function of the temperature only, (it is assumed that there is an excess of hydride present within the tubes vessel, which is always the case) and therefore, generally speaking, it is most advantageous to have deposits of hydride on those surfaces of the tube which are heated to the highest temperature at the very beginning of the operation of the tube, i. e., the cathode structure disclosed in Fig. 2, as long as the element of the structure does not normally rise above the desired temperature required for attaining the optimum pressure. When cathode elements are used for heating the hydride, the gas-pressure inertia of the tube is at a minimum, and the hydrogen pressure may be restored during the initial operating cycle of the tube in the shortest possible time.

connected to the pump. After this operation barium and strontium carbonates deposited on the inner surface of the cathode cylinder 26 and the vanes are converted tothe oxides, by heating the cathode to 1000 C. slowly by means of heating coil 28.

3. All metal parts are heated by induction to a temperature of approximately 900 C. The cathwhose operating temperatures are lower than the temperature of the cathode cylinder.

merits may be the internal heat shields. 37, 34 and gen within the vessel.

' to a source of power.

ode 25 is heated to a temperature of approximately 1000 C. by connecting the heater coil 28 Liquid air is applied to the trap of the vacuum pump for condensing any mercury vapor. This operation is continued for approximately ten minutes.

4. The glass vessel H3 is then filled withhydrogen gas to a pressure in the order of cms. and the metal parts are inductively heated to 1000 C. whereupon they are allowed to cool. The nickel parts of the tube absorb hydrogen during the cooling process, and this absorption of hydrogen results in the lowering of the pressure of hydro- The hydrogen pressure is not allowed to drop below 600 microns.

5. With the hydrogen pressure maintained at 600 micronathe tube is operated with an alternating current source 300, Fig. 3, connected between the cathode and the anode, with the grid of the tube connected to the anode, resistances 3G2 and 304 being inserted in the grid and plate circuits of the thyratron. These resistances, as well as the potential of source 300, are adjusted softhat meter 306 gives an indication of three amperes space current from both the grid and the anode. With the tube operated in this manner and the vessel of the tube connected to a source of hydrogen 308, Fig. 3, the hydrogen pressure is maintained constant until no further hydrogen is absorbed or released by the elements of the tube.

6. The vessel is then sealed-off at 600 microns hydrogen pressure while the tube is operated.

With the above-mentioned procedure applied to the mega-watt thyratron, sufficient hydrogen will be absorbed by the deposited zirconium layers of the thyratron so as to maintain the hydrogen pressure constant during the normal operating conditions of the tube, the ambient temperature within the glass Vessel and the temperature of the metal parts being the factors determining the ambient pressure of the free hydrogen within the vessel. It is to be noted that the hydrogen pressure, because of the continued absorption of hydrogen by the deposited layers of zirconium, will be lower than 600 microns when the tube is cold, the pressure dropping to a few microns at room temperature. When the tube is turned on and heater coil 28 heats the cathode and the adjacent shields, there is a sufficient liberation of hydrogen from the heated parts of the cathode and the shields for restoring the hydrogen pressure to normal with the result that the tube starts operating in the normal manner.

The mechanism of the hydrogen-filled thyratron provided with the deposited layers of hydride, which acts as a reservoir of hydrogen, is therefore as follows:

' The elements of the tube are constructed of any suitable metal, preferably nickel. The nickel surface or surfaces which are known to reach the desired temperatures during the normal operating cycle of the tube are then coated with the physical or chemical hydride whereupon the tube is subjected to the de-gassing and hydrogenation procedure outlined above. In this case'zirconium hydride acts as a hydrogen reservoir and nickel acts, in the main, as the structural and current carrying elements of the tube, the use of nickel for the structural elements rather than of zirconium being preferable because of the brittleness of the zirconium hydride.

The invention thus far has been described specifically in connection with zirconium hydride, however, additional metallic hydrides of the second class and alkali or alkaline earth hydrides of the first class are also suitable for this purpose and therefore, as mentioned previously, the structural elements of the tube may be also coated with the hydrides of barium, strontium, calcium, which form chemical hydrides of the first class and. titanium, thorium, uranium and tantalum, which form physical hydrides of the second class. 7

It should be also stated here that the invention is not limited to the use of any particular element alone as a source of hydrogen, since it is apparent from the given description that the mixtures and alloys of these elements may be also used for accomplishing the sought result.

In determining thetype of hydride to be used, the main factors determining the choice of reservoir element or material are:

1. Characteristics of the desired tube. The required optimum hydrogen pressure within the tubes are controlled by the rated. capacities and the geometry-of the elements but only certain hydrides, chemical ,or physical, could be usedto 10 give that optimum hydrogen pressure, which is dependent on the hydrides equilibrium decomposition pressure, which in itself is dependent on temperature. In other words, the characteristics of the desired tube determine what hydrides can be used because the various hydrides have diiferent equilibrium dissociation pressures at a given temperature. I

2. Ease and rate of approaching the ultimate equilibrium pressure required for good tube performance, this factor, as stated before also including the temperature range; the required temperature for producing the optimum pressure should be sufficiently removed from the ambient temperature variations so that the ambient temperature variations may not produce a marked effect on the pressure.

3. Physical or chemical stability of hydride, which determine such factors as case of manufacture, use, reliability, etc.

In Figs. 1 through 5 one or several of the operating elements of the tube are used as heating elements for the hydrides. Since the equilibrium decomposition pressur of the hydrides is dependent on temperature, it follows that the heating element must possess proper temperature for obtaining optimum hydrogen pressure, and this temperature must remain, during the operating cycle of the tube, substantially constant for maintaining the hydrogen pressure constant. These conditions are attainable in the majority of the cases, since it is quite as important to keep the temperature of the electron-emissive surface of the cathode constant in all thermionic tubes for maintaining constant their operating characteristics. Nevertheless, when the load conditions and the geometry of the tube are apt to produce temperature fluctuations which can not be neglectedand there is a concomitant variation in the pressure of hydrogen, the hydrogen supply problem may be solved in the manner illustrated in Figs. 6 through 9.

In Figs. 6 through 9 the heating element for the hydride is an independent heating element whose cross-sectional view is illustrated in Fig. 7. The entire assembly illustrated in Fig. 7 will be called a hydride capsule.

Referring to Fig. '7, the capsule consists of a cylindrical heat shield 100, an aluminum oxidecoated heater coil H12 mounted on a hydride container 104 coaxially positioned within the heater shield I00, two end-bafiles I96 and 188, an insulating bushing H0, and nickel plugs H2 and H4. The heater is assembled as follows: The hydride container 104, which is a nickel tube approximately inch in diameter, is filled with hydride H6, with plug H4 inserted into the tube, this plug acting as a means for plugging up one end of the tube. After filling the tube with the hydride the right end, which is end H8, of the tube is squeezed together, as illustrated in the drawing, so that the hydride can not fall out of the tube during its subsequent manipulation. A nickel plug H2 is spot-welded to bafile 7B6 whereupon nickel tube Hi l is slipped with its left end over plug H2 and pushed up snugly against bafiie 106 whereupon tube Hi l is cross-welded to plug H2. The squeezed and plugged ends of tube 104 are not welded; since hydrogen penetrates very minute openings the various joints provide adequate connecting channels from the hydride container to the remainder of the gas-filled tube. The heater coil 182 is then slipped over tube 104 and the left end of the coil is welded at 72!] to bafile 106, the welded end of the coil being tion into the vessel of the tube.

grounded. The other end 'of the coil, which is end 122, is slipped through an opening in bushing H which insulates the heater coil from bafiie 108. To accomplish this, ballle 708 is inserted in shield 100, and shield 100 is then slipped over the flanges of baffle E00 whereupon the flanges of the baffle and th shield are welded together as illustrated in the figure.

The capsule is now ready for its mounting in the thyratron, its position in the thyratron being illustrated in Fig. 6. As in the case of Fig. 1, the thyratron includes a glass vessel l 0, an anode lead-in conductor it, an anode supporting glass stem i l, a grid element 56, a grid supporting outer cylinder l9, and a plurality of supportin rods and lead-in conductors embedded in a press 23 of the lower glass-seal cylinder 53 of the tube. The glass vessel, as usual, is mounted on a base The glass stem 53 is provided with a metallic strap 52 and the hydride capsule 100 is mounted directl above strap 53 which supports it by means of rods 602, 003 and 604, the rods 502 and 603 being welded to strap 53 with their lower ends and to the lower portion of cylinder 700 with their upper ends. The outer ungrounded conductor 122 of the heater is connected by means of a lead-in conductor 606 to a prong 508, this prong being also connected through a lead-in wire M0 to the heater coil of the cathode. The heater coil is not illustrated in Fig. 6 but it is identical in all respects to coil 28 illustrated in Fig, 2. Thus the heater 0011 T02 of the capsule is connected directly across the heater coil of the cathode, prongs BIZ and 6M being the two grounded prongs of the thyratron. The circuit of the heater coil of the capsule in Fig. 6 is therefore as follows: a source of potential connected to prong 003, conductor 606, lead-in wire 122, coil E02, baflle I06, shield 100, rods 602 and 663, strap 52, rod 004, cylindrical shield l9, grounded rods 36 and 41, and grounded prongs H2 and 6M. This connection is illustrated more clearly in Fig. 8; a more versatile connection is illustrated in Fig. 9. The resistance of the heater coil 502 is adjusted to heat up the hydride to that temperature which will maintain proper hydrogen pressure in the thyratron, this hydrogen being liberated by the heated hydride H6 inserted in tube 106. In Fig. 9 the lead-in wires Q00 and 002 of heater coil 702 are brought out to independent prongs, and the resistance of the heater coil may be controlled externally by means of a rheostat 904. Thus in Fig. 9 the hydrogen pressure may be controlled at will by rheostat 906. As an example, when barium hydride or zirconium hydride is used, the following dissociation takes place:

BaHz Heat Be H2 Zr-H, Heat Zr +2112 Q' The reaction is a reversible one so that upon cooling there is a reabsorption of hydrogen by barium or zirconium. The physical state of the barium or zirconium metal of course determines the rate of reabsorption. Barium hydride is a good source of hydrogen as it may be seen from the dissociation curves illustrated in Figures 10, 11, 12 and 13. However it is unstable in air since it absorbs and reacts with moisture and thereby decomposes according to the following reaction:

, BaH2+H20 BaO+2H2 Accordingly it may be used only if proper precautions are taken in its handling prior to its inser- Zirconium hydride does not sufier from this disadvantage and 12 therefore its handling prior to its insertion into the tube is easier than that of barium hydride, the dissociation curve of zirconium hydride is illustrated in Fig. 14.

Fig. 10 illustrates theoretically computed dissociation curves for barium, strontium, and calcium hydrides. The calculations were based on thermodynamic free-energy and heat-content values given in the literature.

Fig. 11 illustrates a family of the dissociation curves for barium hydride which were obtained in the following manner:

Curve #1 was obtained by setting a thermocouple into barium hydride sample which itself was inserted in a tube similar to tube I04 illustrated in Fig. '7. The tube was then inserted in a glass vessel and the vessel pumped out. It was then heated for hour at 450 C. with the vessel connected to the pump. The temperature of the glass vessel was then raised to 600 C. and filled with hydrogen to a pressure of 5 mm. and this pressure was maintained within the vessel for hour. Next, with the temperature lowered to 300 C., the vessel was pumped out to hard vacuum, the pumping schedule being continued for hour. The vessel was then sealed-off, allowed to cool and temperature vs. pressure curve #1 obtained by gradually raising the temperature of the glass vessel and of the barium hydride capsule contained in the vessel. The temperature of barium hydride within the capsule was measured by means of the previously mentioned thermocouple inserted in barium hydride, and it was this temperature that was used for plotting the curve.

Curves 2, 3, 4 and 5 were obtained by following the schedules which were as follows:

Curve #2:

1. Pumping for hour at 450 C.

2. Temperature raised to 600 C., hydrogen pressure maintained at 1 centimeter and the pumping continued for hour.

3. Temperature lowered to 300 C. and the pumping continued for hour.

4. The vessel was then sealed-off and the dissociation-curve run made.

Curve #3:

1. Temperature raised to 450 C. and pumping continued for V2 hour.

2. Temperature raised to 600 C., hydrogen pressure maintained at 1 centimeter for hour.

3. Temperature lowered to 300 C. (the source of hydrogen gases connected) and the vessel pumped to hard vacuum for hour.

4. Dissociation curve run made.

Curve #4, same as curve #3 above.

Curve #5:

1. Temperature raised to 450 C. and the vessel pumped to hard vacuum for hour.

2. Temperature raised to 600 C. hydrogen pressure maintained at 1 centimeter for hour.

3. The hydrogen source disconnected, the vessel temperature raised to 450 C. and pumped to hard vacuum for hour.

4. The dissociation curve run made.

Curve #6:

1. Temperature raised to450 C. and the vessel pumped to hard vacuum over a period of hour.

2. The dissociation curve run was made.

Comparison of the curves 1 through 5 with that of curve 6 indicates clearlythat there is some association or absorption of hydrogen by the samples of barium used in the dissociation curve runs which obviously indicates that hydrogen treatment of the barium hydride is desirable if one wishesto obtain the desired gas pressures in a thyratron at lower temperatures. Since the desired working hydrogen pressure in the thyratron under consideration is in the order of 600 microns the curves illustrated in Fig. 11 indicate that the temperature of the hydrides should be in the order of 630 C.

The theoretical curves illustrated in Fig. 10 do not agree with the curves in Fig. 11 which is probably due to the fact that there maybe differences in the techniques and apparatuses used; remoteness from equilibria may exist which may depend on the physical state of the material as well as on the design of the apparatus; and other unpredictable surface phenomena may enter to cause discrepancies.

Fig. 12 illustrates a family of curves which were obtained by inserting the capsule similar to that illustrated in Fig. 7 filled with difierent samples of barium hydride, and measuring the power input dissipated in the heater coil such as heater coil 102, Fig. 7. The hydrogen pressure runs were obtained by first evacuating the vessel to hard vacuum and baking the apparatus at 450 C. while continuing with the pumping schedule for /2' hour; the temperature was then raised to 600 C. and the pumping schedule continued for hour while the vessel was filled with hydrogen and the hydrogen pressure maintained at 5 millimeters through-out the run; the hydrogen source was then disconnected and the pumping schedule continued for an additional /3 hour with the temperature remaining at 450 C. whereupon the glass vessel was sealed-off and the pressure vs. power curves obtained. The curves of Fig. 12 illustrate that a power input in the order of to 12 Watts is required for maintaining the desired hydrogen pressure in the vessel of the megawatt thyratron. The following de-gassing and hydrogenation schedule gives good results when applied to the megawatt thyratron tubes of the type illustrated in Fig. 6, i. e., which use the capsule as a source of hydrogen:

1. Glass vessel is pumped out to hard vacuum.

2. Baking is continued for hour at 450 C. l

with the vessel connected to the pump.

3. With the vessel filled with hydrogen to a pressure of 2 mm., the metal parts of the tube which are above the press 23, Fig; 6, are heated by induction method to 800 0., and this temperature maintained for two minutes with the vessel connected to the pumps. The capsule remains relatively cool because it is below the effective heating field of the induction coil.

Cathode is converted by heat from heater coil 28. Cathode carbonates of barium and strontium are converted into barium and strontium oxides by heat from coil 28.

4. The metal parts of the tube then are degassed by raising the temperature of the parts which are above the glass press 23, Fig. 6, to 900 C. maintaining this temperature for 10 minutes while the glass vesselis connected to the vacuum pumps. Cathode is maintained at 1000" C. by means of additional heat from its heater coil 28. During this operation the capsule remains relatively cool since the induction method is used for heating the upper metal parts of the tube which does not reach the capsule.

5a. The metal parts of the tube above the glass press 23 are inductively heated to 800 C. while the cathode is heated to 900 C. by connecting its heater coil to a source of power and the heating process is continued for two minutes in an atmosphere of hydrogen whose pressure is maintained at 2 mm. while the vessel is connected to the vacuum pumps.

b. Same as Ed but with the source of the external free hydrogen disconnected and tube pumped to a hard vacuum.

0. Same as 5a.

d. Same as 5b. 7

6. The vessel is then filled with hydrogen to a pressure of 600 microns while the tube is still hot and the heat is then shut off.

7. The tube is then operated from an alternating current source with the combined grid plate current equal to approximately 3 amperes and such operation continued for 20 minutes. The schematic diagram of suchoperation of the tube is illustrated in Fig. 3.

8. The tube is then pumped out to hard vac.- uum, the pumps are disconnected, and the heater of the capsule is then connected to the rated source of voltage which produces, because of the hydrogen liberated by the hydride, a hydrogen pressure of 600 microns.

9. The tube is then again operated from an A. C. source as in-7.

10. ,The tube is then allowed to cool and the hydrogen pressure within the vessel, because of its reabsorption, goes to zero.

11a. The vessel is filled with hydrogen up to 600 microns and sealed-oif.

b. The vessel is then sealed-off under Vacuum.

The alternative procedures suggested in 11 produce the following results: When free hydrogen up to the pressure of 600 microns is introduced into the tube prior to its sealing, the time lag experienced during the starting of the tubeis somewhat shorter than in the case when the tube is sealed-off in a vacuum. This time lag is due to the calorific inertia of the capsule.

This phenomenon is illustrated in Fig. 13 in which hydrogen pressure vs. time curves #1 and #2 are illustrated for the megawatt thyratron with barium hydride in the capsule, 11 watts dissipated in the heater coil I02, andtube turned on when 0001 (room temperature). Both curves illustrate the rise of hydrogen pressure in the vessel of the thyratron when the tube was turned on with the initial temperature of the tube equal to room temperature. Curve #1 is for a thyratron sealed-off under vacuum. A maximum pressure of approximately 750 microns was obtained after 2 minutes operation of the heater in the capsule because with the thyratron sealed under vacuum, as stated in 11b, initially there is no hydrogen gas present within the vessel, and, therefore, initially there is no cooling of the capsule by convection, the heat losses being restricted mainly to the heat losses by radiation. The temperature of the capsule thus rises initially to the temperature which is highe than normal operating temperature with the concomitant liberation of excess hydrogen. This higher pressure of hydrogen causes the capsule to be cooled by convection and the hydrogen pressure drops below the normal level. The calorific oscillatory cycle ceases after 6 minutes, and the hydrogen pressure reaches an equilibrium stage.

Curve #2 is a similar curve for the thyratron which was sealedoff with 600 microns hydrogen pressure exerted by the free hydrogen, as described in 11a.

Comparison of the two curves demonstrates the fact that it is preferable to seal the Vessel with the free hydrogen introduced into the vessel since it has a smaller initial calorific inertia than the thyratron sealed at vacuum.

Figs. 14 and 15 disclose typical experimental hydrogentemperature curves for zirconium and titanium hydrides. A chemically pure powdered ziconium (Foot Mineral Company) was used for obtaining zirconium curve illustrated in Fi 14. The experimental procedure for. obtaining this curve was as follows:

1. The vessel of the tube was pumped out with a freeze trap in the line and then out-gassed at 1000 C. for /2 hour,

2. It was then cooled and filled with hydrogen to a pressure of one centimeter,

3. The vessel was then heated to 1000 C., held at 1000 C. for 15 minutes, allowed to cool to room temperature and then pumped out,

4. Dissociation determinations thereafter.

In the case of titanium, a titanium hydride were made '(TiHz made by Metal Hydrides Corporation) was used as a source of hydrogen. The experimental curves were obtained by using the following pro cedure:

1. The vessel was pumped out and a liquid air trap used for freezing out any vapor,

2. The vessel was heated to 450 C. and pumped out to a pressure of approximately 3 microns,

3. Experimental hydrogen pressure temperature determinations were obtained.

Similar curves were also obtained for other hydrides discussed in the specification and they are not furnished 'to avoid undue burdening of the disclosure. These curves were used for determining the best utilization 'of the hydrides as a hydrogen reservoir for the thyratrons. From known temperatures of the elements of the contemplated tube (determined in an experimental tube) and the desired pressure within the vessel of the tube for normal operating conditions, these curves at once furnish the information fo depositing the hydrides on that element ,of the tube which gives the necessary hydrogen pressure within the vessel. 'In the case of the capsules; a curve similar to those illustrated in Fig. 12 is used for determining the wattage that must be used for maintaining the desired hydrogen pressure within the tube. The amount of hydride to be used iscomputed from the quantity of gas requiredv to give the desired pressure within the envelope of the tube at the required dissociation temperature. Ordinarily larger amounts of hydride than the calculated amount is used in order to insure an excess of hydride within the vessel. This excess insures the fact that constant hydro gen pressur is maintained within the vessel as long as the temperature of hydride remains constant.

From the examination of the hydride curves one can readily see that the selected hydrides (including those whose dissociation curves have not been included among the figures) furnish the desired hydrogen pressure when they are heated to the range of temperatures which is in the order of from 400 C. to 600 C. which is a temperature range removed sufiiciently from any ambient temperatures so as to separate sufficiently the effect of artificial heating of the hydrides from the fluctuations of the ambient temperatures. It is to be noted that the ambient temperatures may have some minor efiect on the thyratrons of this type but these efiects now have been minimized to such an extent that they do not represent a source of practical difliculties for preventing operation of the thyratrons at their optimum operating conditions. When" the source of hydrogen is the heated capsule and the circuit of the heated capsule is of the type illustrated in Fig. 9, any adverse effect of the ambient temperatures, which is exhibited in varying heat losses, may be very readily compensated for by adjusting rheo stat 904. Thus the hydrogen pressure may be maintained constant irrespective of the ambient temperature by adjusting the power dissipated in the capsule.

While the invention has been described with reference to several particular embodiments, it will be understood that various modifications of the apparatus shown may be made within the scope of the following claim.

We claim:

A hydrogen filled thermionic tube having a reservoir of tantalum hydride and means for heating said reservoir formaintaining hydrogen pressure within said tube.

' GERARD J. REILLY.

WILLIS E. HARBAUGH.

N 0 references cited. 

